Complications from Use of Sodium Hyaluronate (Healonid) in Anterior Segment Surgery

Total Page:16

File Type:pdf, Size:1020Kb

Complications from Use of Sodium Hyaluronate (Healonid) in Anterior Segment Surgery Br J Ophthalmol: first published as 10.1136/bjo.66.11.714 on 1 November 1982. Downloaded from British Journal ofOphthalmology, 1982, 66, 714-716 Complications from use of sodium hyaluronate (Healonid) in anterior segment surgery S. P. B. PERCIVAL From Scarborough Hospital SUMMARY Sodium hyaluronate brings an important new advance to several techniques in ophthalmic microsurgery. Its use in 226 primary lens implantations is described, and it has been found to be safe and beneficial to both surgeon and patient. Apart from a one day rise of intraocular pressure, obviated by the routine use of timolol maleate or acetazolamide, it has been found in the dosage used to be free from complication. Sodium hyaluronate was first used in ophthalmic and in the field of lens implantation' '3 (anterior surgery as a vitreous substitute more than 10 years chamber manipulation, protection of endothelium, ago' when its properties were shown to be elastic, synechiolysis, iris suturing, and to maintain anterior highly viscous, yet nontoxic, noninflammatory, and chamber depth for secondary procedures such as copyright. nonantigenic.2 More recently Balazs, Miller, and keratoplasty and filtration surgery). Healonid may Stegmann introduced its use into anterior segment also be used in retinal detachment surgery'415 (for surgery.35 The 1% solution (Pharmacia UK Ltd, internal tamponade). Healonid) is at least 400000 times more viscous than This communication seeks to assess the possible aqueous yet will pass through the fine Rycroft complications that may be attributed to Healonid in cannula. It is totally transparent, and because of its the field of primary lens implantation. high molecular weight it is nonosmotic. Because of these properties and the fact that it will maintain Material and methods http://bjo.bmj.com/ anterior chamber depth when air may not, it has been described as the ideal medium for closed chramber Three hundred and thirty-four consecutive lens surgery.6 replacements were performed during the 29 months The particular assets of Healonid are that it will commencing January 1980. 244 followed planned allow complex surgical manipulation in the anterior extracapsular nucleus extraction (as described chamber, improving visibility while protecting the previously6) with an age range 39-88, mean 73 years; corneal endothelium and surrounding tissues from 90 followed intracapsular cryoextraction after on September 25, 2021 by guest. Protected the trauma of surgical instrumentation. It may also be zonulysis, with an age range 56-94, mean 77 years. used to aid atraumatically the cleavage of iris Healonid was used for every case when it was synechiae or other adherent tissues. Thus Healonid available. For standardisation, between 0-2 ml and has a place in the field of trauma'8 (synechiolysis, 0-3 ml was used per eye whether or not the particular extraction ofcorneal splinters penetrating the anterior eye needed it. There was therefore no patient chamber, anterior segment reconstruction), in selection for the use of Healonid. No attempts were keratoplasty459 (both for donor and recipient eye to made to aspirate Healonid at the end of surgery. It protect endothelium), in filtration surgery' (to prevent was used in a total of 226 eyes to deepen the anterior flat anterior chamber and hypotonia), in extra- chamber prior to lens implantation. Of these, 164 capsular cataract extraction'6 (during capsulectomy followed extracapsular extraction when it was also and to protect endothelium from a hard lens nucleus), used to maintain the anterior chamber during capsu- lectomy and inserted to provide a cushion between lens Correspondence to S. P. B. Percival, FRCS, Department of nucleus and cornea during extraction, and 62 Ophthalmology, Scarborough Hospital, Scarborough, North followed cryoextraction, 46 ofwhich also necessitated Yorkshire. an iris suture, placed as described by the author'2 714 Br J Ophthalmol: first published as 10.1136/bjo.66.11.714 on 1 November 1982. Downloaded from Complications from use of sodium hyaluronate (Healonid) in anterior segment surgery 715 Table I Postoperative ocular hypertension in 334 eyes Eves First day Mean IOP (mmHg) IOP>30 mmHg 5 mm>preop. 1st day 3rd day 108 Controls 11(10%) 24(22%) 18-9 15-7 54 Healonid 17 (31%)** 31(57%)** 25 6 15-5 109 Healonid+acetazolamide 8 (7%)** 38 (35%)* 19-7 14-4 63 Healonid+timolol 7 (1 1%)* 20 (32%)* 20-0 14-2 IOP=intraocular pressure. *p<O-0; **p<0-OOl. under Healonid with the chamber closed. There was flow by 33% and tab. acetazolamide 250mgby27%.'7 only one case of aborted lens implantation during the Of the 109 eyes in the present study receiving 29 months, this being for reasons of vitreous loss. Healonid and routine postoperative acetazolamide Postoperative routine included careful slit-lamp the mean first-day intraocular pressure was 19-7 examination by the author on the first, third, and mmHg, and only 7% ofreadings were over 30 mmHg. fifteenth postoperative days and more frequently Of the 63 eyes receiving Healonid and routine timolol when necessary. Raised intraocular pressure was the corresponding figures were 20-0 and 11% treated with topical timolol maleate or systemic respectively. acetazolamide or both in combination. However, These findings confirm the value of acetazolamide following the initial trial with 54 cases, in order to and timolol in reducing aqueous secretion, and Table obviate further ocular hypertension, 2 subgroups of 1 also shows that by the third postoperative day there patients receiving Healonid were made: (a) during was little difference in mean intraocular pressure copyright. 1981 109 patients were given routine intramuscular between the different groups, the marginally higher acetazolamide 500 mg 4 hours after completion of mean pressure found in controls being explained by surgery followed by tablets 250 mg q.d.s. for 2 days; the fact that these eyes were less likely to have been (b) during 1982 63 eyes received timolol maleate offered treatment. 0-25% drops on completion of surgery followed by No significant difference was found between intra- b.d. application for 2 days. Particular attention was capsular and extracapsular eyes (Table 2). There paid to development of uveitis, wound healing, and were no cases of pupil block glaucoma among the ocular hypertension. groups receiving Healonid. http://bjo.bmj.com/ POSTOPERATIVE OCULAR HYPERTENSION Discussion Healonid leaves the anterior chamber by way of the aqueous outflow channels,'6 but the viscosity has to UVEITIS be reduced by dilution with aqueous before this On the first day slit-lamp examination often gives the hydrophilic substance may run through the trabecular appearance of a plastic anterior uveitis in an eye meshwork. Intraocular pressure may rise therefore if containing Healonid. However, this is due to the excessive amounts of Healonid remain in the anterior presence of Healonid holding cells in suspension. on September 25, 2021 by guest. Protected chamber at the end of surgery. Flecks of blood may also be seen held in suspension One hundred and eight eyes did not receive due to rouleaux caused by altered electrostatic charge Healonid or any routine ocular hypotensive. These on red blood cells. These appearances vanish by the acted as controls (Table 1). Of 54 eyes initially third day and do not require specific treatment. 7% of receiving Healonid (all were extracapsular extractions) 57% showed a rise of intraocular pressure 5 mm or Table 2 Incidence ofraised intraocularpressure onfirst more than the preoperative level. The first day postoperative day (the initial 54 extracapsular eyes receiving applanation was over 30 mmHg in 31% and the mean Healonid are excluded) intraocular pressure was 25-6 mmHg compared with IOP>30 mmHg 5 mm>preop. 18-9 mmHg in the control group. Controls28IC 3(11%) 5(18%) Results 80 EC 8(10%) 19(24%) Healonid 62 IC 6(10%) 26(42%) IIOEC 9(8%) 31(28%) In a double-blind trial on 21 normal subjects guttae timolol 0-5% has been shown to reduce the aqueous IOP=intraocular pressure. IC=intracapsular. EC=extracapsular. Br J Ophthalmol: first published as 10.1136/bjo.66.11.714 on 1 November 1982. Downloaded from 716 S. P. B. Percival Healonid eyes and 8% of controls were recorded as References having a more severe uveitis than is expected during I Algrere P. Intravitreal injection of high molecular weight the first postoperative week, but there were no cases hyaluronic acid in retinal detachment surgery. Acta Ophthalmol of hypopyon or of developing keratic precipitates. (Kbh) 1971; 49: 975-7. There were no cases of spluttering hyphaema or of the 2 Balazs EA, Freeman MI, Kloti R. Meyer-Schwickerath G, uveitis-glaucoma-hyphaema (UGH) Regnault F, Sweeney DH. Hyaluronic acid and replacement of syndrome. vitreous and aqueous humour. Mod Probl Ophthalmol 1972; 10: 3-6. WOUND HEALING 3 Balazs EA, Miller D, Stegmann R. Viscosurgery and the use of There were no eyes in which delayed healing or Na-hyaluronate in intraocular lens implantation. Presented at the International Congress and First Film Festival on Intraocular lens improper apposition could be attributed to Healonid. implantation. Cannes, France, May 1979. A disadvantage of Healonid is that at the end of 4 Miller D, Stegmann R. Use of Na-hyaluronate in anterior surgery it is more difficult to assess whether a wound is segment eye surgery. Am Intraoc Implant Soc J 1980; 6: 13-5. water-tight than when the anterior chamber is 5 Pape LG, Balazs EA. The use of Na-hyaluronate in human anterior segment surgery. Ophthalmology 1980; 87: 699-705. reconstituted purely with salt solution. This is of 6 Percival SPB. Protective role of Healon during lens implantation. particular importance during keratoplasty,9 and Trans Ophthalmol Soc UK 1981; 101: 77-8. alternative methods of reconstituting the anterior 7 Stegmann R. Communication to UK Intraocular Implant chamber should be preferred during the final phases Society, Southend, England, May 1981.
Recommended publications
  • Healon®) on a Nonregeneroting (Feline) Corneal Endothelium
    Effect of 1 % Sodium Hyoluronote (Healon®) on a Nonregeneroting (Feline) Corneal Endothelium Charles F. Bahn,* Robert Grosserode,f^: David C. Musch,f Joseph Feder,f§ Roger F. Meyer, f Donald K. MacCallum.f John H. Lillie,f and Norman M. Rich* A series of experiments were performed to investigate the effect of 1% sodium hyaluronate (Healon®) on the nonregenerating corneal endothelium of the cat. Aqueous humor replacement with 1% sodium hyaluronate resulted in mild, transient elevations of intraocular pressure compared to eyes that were injected with balanced salt solution. Sodium hyaluronate 1% protected the feline endothelium against cell loss incurred by contact with hyaluronate-coated intraocular lenses compared to endothelial contact with lenses that were not coated with sodium hyaluronate. The use of intraoperative 1% sodium hyal- uronate, however, did not protect against endothelial cell loss incurred by penetrating keratoplasty or prevent subsequent skin graft-induced corneal homograft rejections. Homograft rejections were milder, however, in some eyes that received grafts coated with 1% sodium hyaluronate. Image analysis of pho- tographs of trypan blue- and alizarin red-stained corneal buttons after trephining, stretching of Descemet's membrane, rubbing against iris-lens preparations, or immediately after penetrating keratoplasty dem- onstrated that the stretching of the posterior cornea is an important cause of endothelial damage that would not be protected against by a viscoelastic coating. Invest Ophthalmol Vis Sci 27:1485-1494,1986
    [Show full text]
  • VISCO-3 (Sodium Hyaluronate)
    Patient Information VISCO-3TM (Sodium Hyaluronate) Federal law restricts this device to sale by or on the order of a physician. Please make sure to read the following important information carefully. This information does not take the place of your doctor’s advice. If you do not understand this information or want to know more, ask your doctor. Your doctor has determined that the knee pain you are experiencing is caused by osteoarthritis and that you are a candidate for a non-surgical, non-pharmacological, pain-relieving therapy called VISCO-3TM. VISCO-3TM is used for the treatment of pain in osteoarthritis of the knee in patients who have failed to get adequate relief from simple painkillers or from exercise and physical therapy. Contents What is VISCO-3TM? 2 What are the benefits of VISCO-3TM? 2 How is VISCO-3TM given? 2 What should you expect following your series of injections? 2 What other treatments are available for osteoarthritis? 3 Are there any reasons why you should not use VISCO-3TM? 3 Possible complications: 3 Other things you should know about VISCO-3 TM: 4 Summary of Clinical Study: 4 How can you get more information about VISCO-3TM? 5 Page 1 of 5 What is VISCO-3TM? VISCO-3TM is a solution made of highly purified, sodium hyaluronate (hyaluronan). Hyaluronan is a natural chemical found in the body and is found in particularly high amounts in joint tissues and in the fluid (synovial fluid) that fills the joints. The body’s own hyaluronan acts like a lubricant and shock absorber in synovial fluid of a healthy joint.
    [Show full text]
  • Management of Joint Disease in the Sport Horse
    1 MANAGEMENT OF JOINT DISEASE IN THE SPORT HORSE Management of Joint Disease in the Sport Horse C. WAYNE MCILWRAITH Colorado State University, Ft. Collins, Colorado INTRODUCTION The joint is an organ, and there are a number of ways in which traumatic damage occurs, ultimately resulting in degradation of articular cartilage. It was recognized in 1966 that articular cartilage change that accompanied osteochondral fragmentation could also be associated with concurrent traumatic damage to the attachment of the joint capsule and ligaments (Raker et al., 1966). However, there was little association made between primary disease in the synovial membrane and fibrous joint capsule and the development of osteoarthritic change in the articular cartilage until an experimental study demonstrated that cartilage degradation could occur in the horse in the absence of instability or trau- matic disruption of tissue and that loss of glycosaminoglycan (GAG) staining was associated with early morphologic breakdown at the surface of the cartilage (McIlwraith and Van Sickle, 1984). Surveys have confirmed that approximately 60% of lameness problems are related to osteoarthritis (National Animal Health Monitoring Systems, 2000; Caron and Genovese, 2003). Rapid resolution of synovitis and capsuli- tis is a critical part of the medical treatment of joint disease because of the principal role of synovitis in causing cartilage matrix breakdown. The goal of treatment of traumatic entities of the joint is twofold: (1) returning the joint to normal as quickly as possible, and (2) preventing the occurrence or reduction of the severity of osteoarthritis. In other words, treatment is intended to (1) reduce pain (lameness), and (2) minimize progression of joint deterioration.
    [Show full text]
  • (HA) Viscosupplementation on Synovial Fluid Inflammation in Knee Osteoarthritis: a Pilot Study
    Send Orders for Reprints to [email protected] 378 The Open Orthopaedics Journal, 2013, 7, 378-384 Open Access Hyaluronic Acid (HA) Viscosupplementation on Synovial Fluid Inflammation in Knee Osteoarthritis: A Pilot Study Heather K. Vincent*,1, Susan S. Percival2, Bryan P. Conrad1, Amanda N. Seay1, Cindy Montero1 and 1 Kevin R. Vincent 1Department of Orthopaedics and Rehabilitation, Interdisciplinary Center for Musculoskeletal Training and Research, 2Department of Food Sciences and Nutrition, University of Florida, Gainesville, FL 32608, USA Abstract: Objective: This study examined the changes in synovial fluid levels of cytokines, oxidative stress and viscosity six months after intraarticular hyaluronic acid (HA) treatment in adults and elderly adults with knee osteoarthritis (OA). Design: This was a prospective, repeated-measures study design in which patients with knee OA were administered 1% sodium hyaluronate. Patients (N=28) were stratified by age (adults, 50-64 years and elderly adults, 65 years). Ambulatory knee pain values and self-reported physical activity were collected at baseline and month six. Materials and Methods: Knee synovial fluid aspirates were collected at baseline and at six months. Fluid samples were analyzed for pro-inflammatory cytokines (interleukins 1, 6,8,12, tumor necrosis factor-, monocyte chemotactic protein), anti-inflammatory cytokines (interleukins 4, 10 13), oxidative stress (4-hydroxynonenal) and viscosity at two different physiological shear speeds 2.5Hz and 5Hz. Results: HA improved ambulatory knee pain in adults and elderly groups by month six, but adults reported less knee pain- related interference with participation in exercise than elderly adults. A greater reduction in TNF- occurred in adults compared to elderly adults (-95.8% ± 7.1% vs 19.2% ± 83.8%, respectively; p=.044).
    [Show full text]
  • Novel Heparin-Like Sulfated Polysaccharides
    ^ ^ ^ ^ I ^ ^ ^ ^ ^ ^ II ^ ^ ^ II ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ ^ I ^ European Patent Office Office europeen des brevets EP 0 940 410 A1 EUROPEAN PATENT APPLICATION (43) Date of publication: (51) |nt CI * C08B 37/08, A61 K 31/73, 08.09.1999 Bulletin 1999/36 A61 K 47/36 A61 1_ 27/00 (21) Application number: 99200468.9 (22) Date of filing: 23.03.1995 (84) Designated Contracting States: • Magnani, Agnese AT BE CH DE DK ES FR GB GR IE IT LI LU MC NL 153010 San Rocco A. Philli (IT) PT SE • Cialdi, Gloria Deceased (IT) (30) Priority: 23.03.1994 IT PD940054 (74) Representative: (62) Document number(s) of the earlier application(s) in Crump, Julian Richard John et al accordance with Art. 76 EPC: FJ Cleveland, 9591 31 58.2 / 0 702 699 40-43 Chancery Lane London WC2A1JQ(GB) (71) Applicant: FIDIA ADVANCED BIOPOLYMERS S.R.L. Remarks: 72100 Brindisi (IT) »This application was filed on 18 - 02 - 1999 as a divisional application to the application mentioned (72) Inventors: under INID code 62. • Barbucci, Rolando »The application is published incomplete (there is no 53100 Siena (IT) claim number 9)as filed (Article 93 (2) EPC). (54) Novel heparin-like sulfated polysaccharides (57) The invention provides sulfated derivatives of jects and pharmaceutical compositions comprising polysaccharides such as hyaluronic acid and hyaluronic these derivatives. The invention further provides for the acid esters exhbiting anticoagulant, antithrombotic and use of these derivatives in the manufacture of pharma- angiogenic activity, for use in the biomedical area. The ceutical compositions, biomedical objects, biomaterials, invention further provides complex ions, biomedical ob- and controlled drug release systems.
    [Show full text]
  • Recent Advances in Equine Osteoarthritis Annette M Mccoy, DVM, MS, Phd, DACVS; University of Illinois College of Veterinary Medicine
    Recent Advances in Equine Osteoarthritis Annette M McCoy, DVM, MS, PhD, DACVS; University of Illinois College of Veterinary Medicine Introduction It is widely recognized that osteoarthritis (OA) is the most common cause of chronic lameness in horses and that it places a significant burden on the equine industry due to the cost of treatment and loss of use of affected animals. Depending on the disease definition and target population, the reported prevalence of OA varies. It was reported at 13.9% in a cross-sectional survey of horses in the UK, but at 97% (defined by loss of range of motion) in a group of horses over 30 years of age. Among Thoroughbred racehorses that died within 60 days of racing, 33% had at least one full-thickness cartilage lesion in the metacarpophalangeal joint, and the severity of cartilage lesions strongly correlated with a musculoskeletal injury leading to death. The majority of the horses in this study were less than 3 years of age, emphasizing the importance of OA in young equine athletes. Unfortunately, a major challenge in managing OA is that by the time clinical signs occur (i.e. lameness), irreversible cartilage damage has already occurred. Although novel treatment modalities are being tested that show promise for modulation of the course of disease, such as viral vector delivery of genes that produce anti-inflammatory products, there are no generally accepted treatments that can be used to reliably reverse its effects once a clinical diagnosis has been made. Thus, there is much research effort being put both into the development of improved diagnostic markers and the development of new treatments for this devastating disease.
    [Show full text]
  • Chondroitin Sulfate/Sodium Hyaluronate Compositions
    ~" ' Nil II II II III III II III MINI Ml J European Patent Office _ © Publication number: 0 136 782 B1 Office europeen* des.. brevets , EUROPEAN PATENT SPECIFICATION © Date of publication of patent specification: 18.03.92 © Int. CI.5: A61 K 31/735 © Application number: 84305221.8 @ Date of filing: 01.08.84 © Chondroitln sulfate/sodium hyaluronate compositions. © Priority: 09.08.83 US 521575 © Proprietor: NESTLE SA Avenue Nestle 55 @ Date of publication of application: CH-1800 Vevey(CH) 10.04.85 Bulletin 85/15 @ Inventor: Chang, Allison S. © Publication of the grant of the patent: 7894 Falrview Road 18.03.92 Bulletin 92/12 Lesage West Virginia 25537(US) Inventor: Boyd, James Edward © Designated Contracting States: Route 1 P.O. Box 135 CH DE FR GB IT LI SE Barbourville West Virginia 25504(US) Inventor: Koch, Harold Otto © References cited: 1017 Big Bend Road Barbourville West Virginia 25504(US) CHEMICAL ABSTRACTS, vol. 98, no. 19, 9th Inventor: Johnson, Richard Michael May 1983, page 44, no. 155193n, Columbus, 905 Woodbine Avenue Ohio, US; S.M. MAC RAE et al.: "The effects Rochester New York 14619(US) of sodium hyaluronate, chondroitln sulfate, and methylcellulose on the corneal endo- thelium and intraocular pressure", & AM. J. Representative: W.P. Thompson & Co. OPHTHALMOL. 1983, 95(3), 332-41 Coopers Building, Church Street Liverpool L1 3AB(GB) 00 CM 00 IV CO CO O Note: Within nine months from the publication of the mention of the grant of the European patent, any person ^ may give notice to the European Patent Office of opposition to the European patent granted.
    [Show full text]
  • Why Chain Length of Hyaluronan in Eye Drops Matters
    diagnostics Review Why Chain Length of Hyaluronan in Eye Drops Matters Wolfgang G.K. Müller-Lierheim CORONIS Foundation, 81241 Munich, Germany; [email protected] Received: 21 June 2020; Accepted: 20 July 2020; Published: 23 July 2020 Abstract: The chain length of hyaluronan (HA) determines its physical as well as its physiological properties. Results of clinical research on HA eye drops are not comparable without this parameter. In this article methods for the assessment of the average molecular weight of HA in eye drops and a terminology for molecular weight ranges are proposed. The classification of HA eye drops according 1 to their zero shear viscosity and viscosity at 1000 s− shear rate is presented. Based on the gradient of mucin MUC5AC concentration within the mucoaqueous layer of the tear film a hypothesis on the consequences of this gradient on the rheological properties of the tear film is provided. The mucoadhesive properties of HA and their dependence on chain length are explained. The ability of HA to bind to receptors on the ocular epithelial cells, and in particular the potential consequences of the interaction between HA and the receptor HARE, responsible for HA endocytosis by corneal epithelial cells is discussed. The physiological function of HA in the framework of ocular surface homeostasis and wound healing are outlined, and the influence of the chain length of HA on the clinical performance of HA eye drops is illustrated. The use of very high molecular weight HA (hylan A) eye drops as drug vehicle for the next generation of ophthalmic drugs with minimized side effects is proposed and its advantages elucidated.
    [Show full text]
  • (Hyaluronic Acid) Promotes Migration of Human Corneal Epithelial Cells in Vitro J a P Gomes, R Amankwah, a Powell-Richards, H S Dua
    821 EXTENDED REPORT Br J Ophthalmol: first published as 10.1136/bjo.2003.027573 on 17 May 2004. Downloaded from Sodium hyaluronate (hyaluronic acid) promotes migration of human corneal epithelial cells in vitro J A P Gomes, R Amankwah, A Powell-Richards, H S Dua ............................................................................................................................... Br J Ophthalmol 2004;88:821–825. doi: 10.1136/bjo.2003.027573 Purpose: Sodium hyaluronate (hyaluronic acid) is known to promote corneal epithelial wound healing in vivo and in vitro, in animal experiments. Sodium hyaluronate is the ligand for CD44, a cell surface adhesion molecule which has been found on normal human corneal epithelial cells. The purpose of this study was to investigate the effect of sodium hyaluronate on human corneal epithelial cell migration, proliferation, and CD44 receptor expression. Methods: Human corneal epithelial cell cultures were established from 32 donor corneoscleral rims and See end of article for maintained separately in three different culture conditions: (1) culture medium only, (2) sodium authors’ affiliations ....................... hyaluronate enriched (0.6 mg/ml) medium, and (3) hydroxypropylmethylcellulose enriched (2.5 mg/ml) medium. The total area of migrating epithelial cell sheets in each case was measured by planimetry on Correspondence to: days 4, 8, 12, and 16. Cytospin preparations of cells cultured in the different culture conditions were Professor H S Dua, Division of Ophthalmology examined immunohistochemically for proliferation and CD44 receptor expression using antibodies and Visual Sciences, B directed against Ki67 and CD44 respectively. Floor, Eye Ear Nose Throat Results: Cells cultured in the presence of sodium hyaluronate showed significantly increased migration at Centre, University days 12 and 16 (Friedmen test: p = 0.0012, day 16; p = ,0.001, day 12) compared with cells cultured in Hospital, Queens Medical Centre, Nottingham NG7 the other media.
    [Show full text]
  • The Use of Sodium Hyaluronate in the Treatment of Temporomandibular
    Rev Dor. São Paulo, 2013 out-dez;14(4):301-6 ARTIGO DE REVISÃO The use of sodium hyaluronate in the treatment of temporomandibular joint disorders* O uso do hialuronato de sódio no tratamento das disfunções temporomandibulares articulares Eduardo Grossmann1, Eduardo Januzzi2, Liogi Iwaki Filho3 *Recebido da Universidade Federal do Rio Grande do Sul, Porto Alegre, RS. ABSTRACT Keywords: Clinical treatment, Nonreducing disk displacement, Osteoarthritis, Reducing disk displacement Sodium hyaloruna- BACKGROUND AND OBJECTIVES: Temporomandibular te, Surgical treatment, Temporomandibular joint, Viscosupple- disorder is a collective term involving clinical masticatory muscles, mentation. temporomandibular joints and/or associated structures changes. This study aimed at reviewing, using major databases, the effective- RESUMO ness and safety of sodium hyaluronate in the treatment of temporo- mandibular joint disorders, aiming at recommending or discarding JUSTIFICATIVA E OBJETIVOS: A disfunção temporomandibu- its clinical use. lar compreende um termo coletivo que envolve alterações clínicas CONTENTS: The following databases were queried: Medline, via nos músculos da mastigação, das articulações temporomandibulares Pubmed (1966-2013), Cochrane Central Registry of Controlled e/ou estruturas associadas.O objetivo deste estudo foi realizar uma Trials (2012), Embase (1980-2013) and LILACS (1982-2013). The análise crítica, utilizando as principais bases de dados, sobre a efe- strategy was a search adjusted to each database to identify the largest tividade e a segurança do hialuronato de sódio no tratamento das possible number of studies involving sodium hyalorunate to manage disfunções temporomandibulares de origem articular, a fim de reco- joint temporomandibular disorders. Language was limited to articles mendar ou refutar seu uso na prática clínica. published in English.
    [Show full text]
  • Hyaluronic Acid Viscosupplementation and Osteoarthritis
    AJSM PreView, published on January 23, 2009 as doi:10.1177/0363546508326984 Basic Science Update Hyaluronic Acid Viscosupplementation and Osteoarthritis Current Uses and Future Directions Eric J. Strauss,* MD, Jennifer A. Hart,† MPAS, PA-C, Mark D. Miller,† MD, Roy D. Altman,‡ MD, and Jeffrey E. Rosen,*§ MD From the *Department of Orthopaedic Surgery, NYU Hospital for Joint Diseases, New York, New York, the †Department of Orthopaedic Surgery, University of Virginia, Charlottesville, Virginia, and the ‡Division of Rheumatology and Immunology, University of California, Los Angeles, Los Angeles, California Intra-articular hyaluronic acid viscosupplementation is gaining popularity as a treatment option in the nonoperative management of patients with osteoarthritis. Recent clinical studies have demonstrated that the anti-inflammatory, anabolic, and chondropro- tective actions of hyaluronic acid reduce pain and improve patient function. With evidence mounting in support of the efficacy of this treatment modality for patients with osteoarthritis, its potential use in additional patient populations and for other patho- logies affecting the knee is being investigated. The current article reviews the use of intra-articular hyaluronic acid viscosupple- mentation in the management of knee osteoarthritis and presents the potential for expanding its indications for other joints and alternative patient subpopulations. Additionally, future directions for the use of hyaluronic acid and areas of active research are discussed. Keywords: hyaluronic acid; viscosupplementation; osteoarthritis; knee With the aging of the “baby boomers,” the prevalence of if possible. Nonoperative treatment options for symptomatic osteoarthritis (OA) in the United States is increasing, with arthritis include lifestyle modifications, physical therapy, recent projections reporting that by the year 2030, almost systemic anti-inflammatory medications, intra-articular 67 million Americans will be affected by the disease.
    [Show full text]
  • Three Pearls for Surgery in Uveitis Patients
    Three Pearls for Surgery in Uveitis Patients Addressing these important questions can help to ensure a positive outcome. BY LISA J. FAIA, MD he main indications for surgical intervention for traction as a “third hand” to create countertraction for patients with uveitis are the same as those for any further delamination of membranes. patient: to correct a visually significant or vision- Sodium hyaluronate is a useful tool for countertraction, threatening etiology. Additionally, interventions as it shows the location of the remaining retinal contraction may be helpful to elicit a diagnosis or as a form of and it can be easily removed, even if it goes subretinal. Tinflammatory control. In uveitic patients, bleeding is the enemy, even more so The keys to success with any surgery include a thorough than in noninflammatory detachments. The inflammation preoperative evaluation, an accurate diagnosis, a proper is an issue, and hemostasis must be achieved (Figure). To surgical plan, and a meticulous approach. For surgery in watch a successful retinal detachment repair in a patient patients with uveitis, additional steps include good preopera- with uveitis, visit bit.ly/FAIA1. tive control of the inflammation and a plan for escalation of inflammatory control before surgery to better ensure suc- HOW QUIET DOES THE EYE HAVE TO BE? cess. Postoperatively, surgeons must be ready to recognize, as In an ideal world, the eye would be completely quiet— early as possible, any reactivation of inflammation and treat meaning no cell, haze, macular edema, vasculitis, etc.—for it to ensure that it does not escalate beyond control. 3 full months prior to surgery.
    [Show full text]